Canonical Allele Identifier: CA2672441663

Gene: FGB

Linked Data

• gnomAD v4: 4-154569782-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569786_154569787del , CM000666.2:g.154569786_154569787del	GRCh38
NC_000004.11:g.155490938_155490939del , CM000666.1:g.155490938_155490939del	GRCh37
NC_000004.10:g.155710388_155710389del	NCBI36
NG_008833.1:g.11807_11808del , LRG_558:g.11807_11808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1231_1232del MANE Select	ENSP00000306099.4:p.Asp411GlnfsTer2
ENST00000302068.8:c.1231_1232del	ENSP00000306099.4:p.Asp411GlnfsTer2
ENST00000502545.5:n.939+479_939+480del
ENST00000509493.1:c.574_575del	ENSP00000426757.1:p.Asp192GlnfsTer2
NM_001184741.1:c.1054_1055del	NP_001171670.1:p.Asp352GlnfsTer2
NM_005141.4:c.1231_1232del , LRG_558t1:c.1231_1232del	NP_005132.2:p.Asp411GlnfsTer2
NM_001382759.1:c.1099_1100del	NP_001369688.1:p.Asp367GlnfsTer2
NM_001382760.1:c.1231_1232del	NP_001369689.1:p.Asp411GlnfsTer2
NM_001382761.1:c.1231_1232del	NP_001369690.1:p.Asp411GlnfsTer2
NM_001382762.1:c.931_932del	NP_001369691.1:p.Asp311GlnfsTer2
NM_001382763.1:c.1222_1223del	NP_001369692.1:p.Asp408GlnfsTer2
NM_001382764.1:c.*5_*6del	NP_001369693.1:n.*5_*6del
NM_001382765.1:c.1220+11_1220+12del	NP_001369694.1:n.1220+11_1220+12del
NM_005141.5:c.1231_1232del MANE Select	NP_005132.2:p.Asp411GlnfsTer2